Page last updated: 2024-10-31

nocodazole and Fragile X Syndrome

nocodazole has been researched along with Fragile X Syndrome in 1 studies

Fragile X Syndrome: A condition characterized genotypically by mutation of the distal end of the long arm of the X chromosome (at gene loci FRAXA or FRAXE) and phenotypically by cognitive impairment, hyperactivity, SEIZURES, language delay, and enlargement of the ears, head, and testes. INTELLECTUAL DISABILITY occurs in nearly all males and roughly 50% of females with the full mutation of FRAXA. (From Menkes, Textbook of Child Neurology, 5th ed, p226)

Research Excerpts

ExcerptRelevanceReference
"Lack of fragile X mental retardation protein (FMRP) causes fragile X syndrome, a common form of inherited mental retardation."1.31Transport of fragile X mental retardation protein via granules in neurites of PC12 cells. ( De Diego Otero, Y; Oostra, B; Schrier, M; Severijnen, LA; van Cappellen, G; Willemsen, R, 2002)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
De Diego Otero, Y1
Severijnen, LA1
van Cappellen, G1
Schrier, M1
Oostra, B1
Willemsen, R1

Other Studies

1 other study available for nocodazole and Fragile X Syndrome

ArticleYear
Transport of fragile X mental retardation protein via granules in neurites of PC12 cells.
    Molecular and cellular biology, 2002, Volume: 22, Issue:23

    Topics: Animals; Anti-Bacterial Agents; Antineoplastic Agents; Cytochalasin D; Cytoplasmic Granules; Doxycyc

2002